Homo sapiens (human): 4654
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Entry
4654 CDS
T01001
Symbol
MYOD1, CMYP17, MYF3, MYOD, MYODRIF, PUM, bHLHc1
Name
(RefSeq) myogenic differentiation 1
KO
K09064
myogenic factor 3
Organism
hsa
Homo sapiens (human)
Pathway
hsa05017
Spinocerebellar ataxia
Disease
H01810
Congenital myopathy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09164 Neurodegenerative disease
05017 Spinocerebellar ataxia
4654 (MYOD1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
4654 (MYOD1)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Basic helix-loop-helix (bHLH)
Myogenic transcription factors
4654 (MYOD1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Basic
Myf5
HLH
Motif
Other DBs
NCBI-GeneID:
4654
NCBI-ProteinID:
NP_002469
OMIM:
159970
HGNC:
7611
Ensembl:
ENSG00000129152
UniProt:
P15172
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All DBs
Position
11:17719571..17722136
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AA seq
320 aa
AA seq
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MELLSPPLRDVDLTAPDGSLCSFATTDDFYDDPCFDSPDLRFFEDLDPRLMHVGALLKPE
EHSHFPAAVHPAPGAREDEHVRAPSGHHQAGRCLLWACKACKRKTTNADRRKAATMRERR
RLSKVNEAFETLKRCTSSNPNQRLPKVEILRNAIRYIEGLQALLRDQDAAPPGAAAAFYA
PGPLPPGRGGEHYSGDSDASSPRSNCSDGMMDYSGPPSGARRRNCYEGAYYNEAPSEPRP
GKSAAVSSLDCLSSIVERISTESPAAPALLLADVPSESPPRRQEAAAPSEGESSGDPTQS
PDAAPQCPAGANPNPIYQVL
NT seq
963 nt
NT seq
+upstream
nt +downstream
nt
atggagctactgtcgccaccgctccgcgacgtagacctgacggcccccgacggctctctc
tgctcctttgccacaacggacgacttctatgacgacccgtgtttcgactccccggacctg
cgcttcttcgaagacctggacccgcgcctgatgcacgtgggcgcgctcctgaaacccgaa
gagcactcgcacttccccgcggcggtgcacccggccccgggcgcacgtgaggacgagcat
gtgcgcgcgcccagcgggcaccaccaggcgggccgctgcctactgtgggcctgcaaggcg
tgcaagcgcaagaccaccaacgccgaccgccgcaaggccgccaccatgcgcgagcggcgc
cgcctgagcaaagtaaatgaggcctttgagacactcaagcgctgcacgtcgagcaatcca
aaccagcggttgcccaaggtggagatcctgcgcaacgccatccgctatatcgagggcctg
caggctctgctgcgcgaccaggacgccgcgccccctggcgccgcagccgccttctatgcg
ccgggcccgctgcccccgggccgcggcggcgagcactacagcggcgactccgacgcgtcc
agcccgcgctccaactgctccgacggcatgatggactacagcggccccccgagcggcgcc
cggcggcggaactgctacgaaggcgcctactacaacgaggcgcccagcgaacccaggccc
gggaagagtgcggcggtgtcgagcctagactgcctgtccagcatcgtggagcgcatctcc
accgagagccctgcggcgcccgccctcctgctggcggacgtgccttctgagtcgcctccg
cgcaggcaagaggctgccgcccccagcgagggagagagcagcggcgaccccacccagtca
ccggacgccgccccgcagtgccctgcgggtgcgaaccccaacccgatataccaggtgctc
tga
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